Influence of recent volcanism of the geochemical behaviour of trace elements and gases in deep granitic hydrothermal systems, southwest Bulgaria

2021 ◽  
pp. 383-387
Author(s):  
E.N. Pentcheva ◽  
L. Van’t dack ◽  
R. Gijbels
Chemosphere ◽  
2020 ◽  
Vol 252 ◽  
pp. 126430 ◽  
Author(s):  
K. Prabakaran ◽  
S. Eswaramoorthi ◽  
R. Nagarajan ◽  
A. Anandkumar ◽  
F. Merlin Franco

2021 ◽  
Author(s):  
Andres Cardenas Niño ◽  
Rosa Marques ◽  
Maria Dias ◽  
Catarina Diamantino ◽  
Edgar Carvalho

2018 ◽  
Vol 59 (12) ◽  
pp. 2148-2165
Author(s):  
V.L. Tauson ◽  
S.V. Lipko ◽  
N.V. Smagunov ◽  
R.G. Kravtsova ◽  
K.Yu. Arsent'ev

2015 ◽  
Vol 87 (4) ◽  
pp. 1959-1979 ◽  
Author(s):  
AKIHISA MOTOKI ◽  
SUSANNA E. SICHEL ◽  
THAIS VARGAS ◽  
DEAN P. MELO ◽  
KENJI F. MOTOKI

ABSTRACT This paper presents geochemical behaviour of trace elements of the felsic alkaline rocks of the state of Rio de Janeiro, Brazil, with special attention of fractional crystallization and continental crust assimilation. Fractionation of leucite and K-feldspar increases Rb/K and decreases K2O/(K2O+Na2O). Primitive nepheline syenite magmas have low Zr/TiO2, Sr, and Ba. On the Nb/Y vs. Zr/TiO2 diagram, these rocks are projected on the field of alkaline basalt, basanite, and nephelinite, instead of phonolite. Well-fractionated peralkaline nepheline syenite has high Zr/TiO2 but there are no zircon. The diagrams of silica saturation index (SSI) distinguish the trends originated form fractional crystallization and crustal assimilation. In the field of SSI<-200, Zr/TiO2 and Ba/Sr have negative correlations to SSI in consequence of fractional crystallization. In the field of SSI>-200, they show positive correlations due to continental crust assimilation. Total REEs (Rare Earth Elements) is nearly 10 times that of granitic rocks, but LaN/SmN and LaN/YbN are similar. REE trend is linear and Eu anomaly is irrelevant. The pegmatitic liquid generated by country rock partial melting is SiO2-oversaturated and peraluminous with high Ba, Sr, Ba/Sr, Zr/TiO2, and SSI, with high content of fluids. This model justifies the peraluminous and SiO2-oversaturated composition of the rocks with relevant effects of continental crust assimilation.


Minerals ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 526 ◽  
Author(s):  
Yejian Wang ◽  
Xiqiu Han ◽  
Sven Petersen ◽  
Matthias Frische ◽  
Zhongyan Qiu ◽  
...  

The ultramafic-hosted Kairei vent field is located at 25°19′ S, 70°02′ E, towards the Northern end of segment 1 of the Central Indian Ridge (CIR-S1) at a water depth of ~2450 m. This study aims to investigate the distribution of trace elements among sulfide minerals of differing textures and to examine the possible factors controlling the trace element distribution in those minerals using LA-ICP-MS spot and line scan analyses. Our results show that there are distinct systematic differences in trace element distributions throughout the different minerals, as follows: (1) pyrite is divided into three types at Kairei, including early-stage euhedral pyrite (py-I), sub-euhedral pyrite (py-II), and colloform pyrite (py-III). Pyrite is generally enriched with Mo, Au, As, Tl, Mn, and U. Pyrite-I has high contents of Se, Te, Bi, and Ni when compared to the other types; py-II is enriched in Au relative to py-I and py-III, but poor in Ni; py-III is enriched in Mo, Pb, and U but is poor in Se, Te, Bi, and Au relative to py-I and py-II. Variations in the concentrations of Se, Te, and Bi in pyrite are most likely governed by the strong temperature gradient. There is generally a lower concentration of nickel than Co in pyrite, indicating that our samples precipitated at high temperatures, whereas the extreme Co enrichment is likely from a magmatic heat source combined with an influence of serpentinization reactions. (2) Chalcopyrite is characterized by high concentrations of Co, Se, and Te. The abundance of Se and Te in chalcopyrite over the other minerals is interpreted to have been caused by the high solubilities of Se and Te in the chalcopyrite lattice at high temperatures. The concentrations of Sb, As, and Au are relatively low in chalcopyrite from the Kairei vent field. (3) Sphalerite from Zn-rich chimneys is characterized by high concentrations of Sn, Co, Ga, Ge, Ag, Pb, Sb, As, and Cd, but is depleted in Se, Te, Bi, Mo, Au, Ni, Tl, Mn, Ba, V, and U in comparison with the other minerals. The high concentrations of Cd and Co are likely caused by the substitution of Cd2+ and Co2+ for Zn2+ in sphalerite. A high concentration of Pb accompanied by a high Ag concentration in sphalerite indicates that Ag occurs as Pb–Ag sulfosalts. Gold is generally low in sphalerite and strongly correlates with Pb, suggesting its presence in microinclusions of galena. The strong correlation of As with Ge in sphalerite from Kairei suggests that they might precipitate at medium temperatures and under moderately reduced conditions. (4) Bornite–digenite has very low concentrations of most trace elements, except for Co, Se, and Bi. Serpentinization in ultramafic-hosted hydrothermal systems might play an important role in Au enrichment in pyrite with low As contents. Compared to felsic-hosted seafloor massive sulfide deposits, sulfide minerals from ultramafic-hosted deposits show higher concentrations of Se and Te, but lower As, Sb, and Au concentrations, the latter often attributed to the contribution of magmatic volatiles. As with typical ultramafic-hosted seafloor massive sulfide deposits, Se enrichment in chalcopyrite from Kairei indicates that the primary factor that controls the Se enrichment is temperature-controlled mobility in vent fluids.


1994 ◽  
Vol 353 ◽  
Author(s):  
David Savage

Abstract59Ni may make significant contributions to calculated doses in performance assessment (PA) studies of geological repositories for radioactive waste, due principally to the adoption of relatively high near-field solubilities. Ni concentration values used in PA are typically 1–6 orders of magnitude greater than those measured in natural groundwaters. This difference is a result of the utilisation in PA of solubility data for pure nickeliferous solids, and in some instances, the selection of solids chemically incompatible with the disposal environment. The geochemical behaviour of Ni is reviewed. It is considered highly unlikely that Ni will form discrete pure solids in the repository near-field, so that partition as a trace element into solid solutions should be considered. Henry’s law behaviour of trace elements is discussed and geochemically-realistic Ni solubility values for HLW and L/ILW disposal scenarios calculated. It is concluded that Ni will behave according to the chemical conditions of the disposal environment, which should be reflected in the choice of solubility data for PA. The adoption of solid solution modelling for other elements of interest to PA should be considered.


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